Withings

About the Company

Withings created the first smart scale in 2009, and has been the pioneer in connected health ever since. Its clinically validated and multi-award winning range is used by millions worldwide, and includes smart scales, hybrid watches, blood pressure monitors, sleep analyzers and more. The team of engineers, data scientists, and healthcare professionals at Withings work alongside clinical experts to make it possible to take medical-grade measurements at home. Withings was the first to bring measurements for pulse wave velocity and electrodermal activity into the home – finding ever more precise ways to measure our health. Each device is designed to fit beautifully into daily life, supported by an app that unlocks long-term health insights and offers programs to create meaningful change. At Withings we’re dedicated to creating a world where people can see their path to better health, and feel supported to pursue it. Find out more at withings.com and connect with us on Facebook, Instagram or Twitter.

Listed Jobs

Company Name

Withings

Job Title

Stage - Assurance Qualité & Affaire Réglementaire Dispositifs Médicaux (H/F)

Job Description

**Job Title** Intern – Quality Assurance & Regulatory Affairs (Medical Devices) **Role Summary** Support the Quality Management System (QMS) for a medical‑device company, ensuring compliance with CE, 510(k) and other regulatory requirements while maintaining ISO 13485 standards. **Expectations** - Deliver accurate, timely technical dossiers and support export/market‑entry approvals. - Demonstrate initiative, flexibility, and a strong sense of ownership in a fast‑changing environment. - Communicate effectively with R&D, sales, and cross‑functional teams in French and English. **Key Responsibilities** - Contribute to obtaining and maintaining CE, 510(k) and other regulatory approvals via complete technical dossiers. - Support R&D and sales teams with quality and regulatory needs. - Maintain and update QMS in response to regulatory and normative changes. - Monitor regulatory developments and manage associated action plans. - Manage documentation control, change control, CAPA processes, and non‑conformity correction. - Assist in preparing and participating in management reviews and internal/external audits. - Facilitate and lead quality training activities to promote a quality culture. - Draft, structure, and review regulatory and quality documentation. **Required Skills** - Strong analytical and problem‑solving abilities. - Excellent written and verbal communication in French and English. - Proficient in document management and CAPA tools. - Ability to work autonomously and in multidisciplinary, multicultural teams. - Detail‑oriented, organized, and capable of meeting tight deadlines. - Knowledge of ISO 13485 and/or EU MDR 2017/ 745 is a plus. **Required Education & Certifications** - Current enrolment in a Bac+4/5 (or equivalent) program in Quality & Regulatory Affairs, Biomedical Engineering, or related field. - No prior certification required; familiarity with ISO 13485 or EU MDR is advantageous.

Issy-les-moulineaux, France

On site

01-10-2025

Company Name

Withings

Job Title

Stage - Assistant.e qualité Dispositifs médicaux H/F

Job Description

**Job title:** Medical Device Quality Assurance Intern **Role summary:** Support the Quality & Regulatory department in maintaining and updating the company’s quality management systems (QMS) for medical devices, in line with ISO 13485, FDA CFR 21 820, and forthcoming regulations such as the AI Act and SaMD standards. Contribute to continuous improvement, audit readiness, and documentation management. **Expectations:** * Assist in the application and enhancement of QMS, ISMS, and PIMS standards. * Analyze nonconformities, propose corrective actions, and track CAPA effectiveness. * Participate in internal and external audits and in the development of ISO 42001 and ISO 62304 compliant procedures and documents. * Communicate and collaborate effectively across multidisciplinary teams. **Key responsibilities:** * Update and maintain quality documentation (procedures, work instructions, forms). * Draft and review quality records in compliance with ISO 13485 and FDA regulations. * Conduct root-cause analyses for nonconformities and support CAPA cycle closure. * Prepare documentation for internal and third‑party audits. * Assist in creating and implementing procedures for AI Act and SaMD applicability. * Contribute to the development of ISO 42001 and ISO 62304‐specific processes. * Gather and translate regulatory requirements into actionable quality actions. **Required skills:** * Strong written and verbal communication in English; ability to produce documents in English. * Proficiency with Google Workspace or Microsoft Office suite. * Analytical mindset and ability to manage multiple tasks concurrently. * Excellent interpersonal skills and teamwork orientation. * Enthusiastic about learning new domains (software, AI, electronics, chemistry, etc.). **Required education & certifications:** * Current student or recent graduate in pharmaceutical sciences, engineering, or a related university program focusing on Quality Assurance or Regulatory Affairs. * Familiarity with ISO 13485 preferred; basic understanding of medical device regulations is an advantage. ---

Issy-les-moulineaux, France

On site

01-10-2025

Company Name

Withings

Job Title

Internship - Data collection - ML (H/F)

Job Description

**Job Title:** Data Collection & Monitoring Intern – Machine Learning (ML) **Role Summary:** Six‑month internship within the Machine Learning Data Engineering squad of a leading connected‑health company. The intern will design, develop, and deploy a full‑stack solution for extracting, aggregating, storing, and visualizing performance metrics from diverse product and algorithm sources to support model validation and continuous improvement. **Expectations:** - Work autonomously while collaborating with cross‑functional teams (ML, validation, hardware). - Translate stakeholder requirements into technical specifications. - Deliver a production‑ready data pipeline, storage schema, and monitoring dashboards within the internship period. - Communicate progress and results clearly in English, both written and verbally. **Key Responsibilities:** 1. Elicit and document precise data‑collection needs from internal users. 2. Architect and implement an end‑to‑end pipeline: API ingestion → data cleaning → storage in relational/NoSQL databases. 3. Develop monitoring tools (e.g., dashboards, alerts) to compare legacy and new algorithm performance. 4. Deploy the solution on Linux environments and ensure scalability and reliability. 5. Promote adoption across teams, provide training, and incorporate feedback for refinements. **Required Skills:** - Proficiency in Python (pandas, requests, etc.). - Familiarity with databases (SQL and/or NoSQL) and API integration. - Basic Linux command‑line experience. - Strong analytical mindset with interest in data engineering, visualization, and health‑tech applications. - Technical English proficiency (reading and writing). - Good written communication, attention to detail, self‑motivation, and teamwork abilities. **Required Education & Certifications:** - Currently enrolled in a Bachelor’s or Master’s program (or equivalent) in Computer Science, Data Engineering, Electrical Engineering, Biomedical Engineering, or a related field. - No specific certifications required; demonstrable coursework or project experience in Python, databases, or data pipelines is expected.

Issy-les-moulineaux, France

On site

09-10-2025

Company Name

Withings

Job Title

Juriste généraliste - Droit des affaires (H/F)

Job Description

**Job Title** Generalist Business Lawyer – Contract & Data Privacy **Role Summary** Provide comprehensive legal support across the organization, focusing on contract drafting, negotiation, and management, while ensuring compliance with personal data protection regulations. Operate in an international, agile environment, contributing proactively to project lifecycles and shaping legal processes. **Expectations** - Work closely with cross‑functional teams (product, sales, supply chain, compliance). - Deliver clear, practical legal guidance that integrates early into product and business initiatives. - Maintain fluent English communication (written & spoken) for regular interactions with international partners. - Embrace modern legal technology (SaaS, legal tech, collaboration tools). - Foster continuous improvement of legal workflows and knowledge sharing. **Key Responsibilities** 1. **Contract Law** - Advise operations on contract analysis, drafting, and negotiation (clients, suppliers, NDAs, distribution agreements). - Manage contract lifecycle using the company’s dedicated tool; track status and drive process optimisation. - Update and create standard contract templates. - Produce internal legal updates and briefing notes. 2. **Personal Data Protection** - Respond to internal privacy inquiries and support data protection governance. - Contribute to the development and delivery of privacy training programs. - Author a regular newsletter on data‑privacy and compliance topics. - Ensure GDPR compliance and maintain awareness of international regulatory developments. 3. **Process & Tool Management** - Champion the structuring and optimisation of legal processes. - Evaluate and recommend legal tech solutions (e.g., document automation, contract management). - Facilitate knowledge transfer and cultivate a collaborative, solution‑oriented culture. **Required Skills** - Expertise in contract law, negotiation, and risk assessment. - Strong knowledge of data protection regulations (GDPR and related frameworks). - Proficient in English (written & spoken) for international collaboration. - Experience with Google Workspace, Notion, and readiness to adopt new SaaS tools. - Analytical mindset, meticulous attention to detail, and excellent communication & teaching abilities. - Proactive, solution‑focused, and comfortable working in fast‑paced, cross‑functional settings. **Required Education & Certifications** - Master’s degree (Master 2) in Business Law, Contract Law, or Digital Law (or equivalent). - Relevant corporate legal experience (internship, apprenticeship, or first professional role).

Issy-les-moulineaux, France

Hybrid

17-11-2025